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Ethylene Glycol Dinitrate (EGDN): from Commercial Precursors, Physicochemical and Detonation Characterization

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Currently, liquid explosives pose a potential threat. An important phase in the assessment of this threat is to investigate the various synthesis paths leading to their manufacture and to evaluate the potential use of readily purchasable precursors. The aim of this work was to assess the synthesis of Ethylene Glycol Dinitrate (EGDN), a liquid nitrate ester explosive, using commercially available precursors. The characteristics of the synthetic process (ease, yield), the chemical properties of the synthesized product (purity, spectra) and its explosive properties (sensitivities, detonability) were investigated. Comparisons are drawn between these products and the product obtained using laboratory ingredients. Three ingredients have been used: 1) ethylene glycol, laboratory grade, 2) ready to use, commercial coolant fluid, and 3) ethylene glycol extracted from commercial coolant fluid. The chemical composition and purity of the synthesized liquid explosive was analyzed by Gas Chromatography-Mass Spectrometry (GCMS), and infrared spectroscopy (IR). Differential Scanning Calorimetric (DSC) analysis allowed the heat of decomposition and activation energies to be assessed. The Ozawa and Kissinger models were used. The explosive properties of the pure synthesized products and comparable other explosives, have been tested. The potential use as a priming charge or as a main charge was assessed.
Rocznik
Strony
287--305
Opis fizyczny
Bibliogr. 20 poz., rys., tab.
Twórcy
autor
  • Royal Military Academy, Department of Chemistry, Laboratory for Energetic Materials, Av. de la Renaissance 30, 1000, Brussels, Belgium
autor
  • Royal Military Academy, Department of Chemistry, Laboratory for Energetic Materials, Av. de la Renaissance 30, 1000, Brussels, Belgium
Bibliografia
  • [1] Beveridge A., Forensic Investigation of Explosives, Taylor & Francis, UK, 2003, 290.
  • [2] National Research Council, Disrupting Improvised Device Report, The National Academies Press, USA, 2008.
  • [3] Akhavan J., The Chemistry of Explosives, RSC, UK, 2004, Ch. 3, p. 52.
  • [4] Meyer R., Köhler J, Homburg A., Explosives, Sixth completely revised ed., Wiley-VCH, Weinheim, 2007.
  • [5] Gouranlou F., Kohsary I., Synthesis and Characterization of 1,2,4-Butanetriol Trinitrate, Asian J. Chem., 2010, 22, 4221-4228
  • [6] Ethylene Dinitrate, Health-based Reassessment of Administrative Occupational, Committee on Updating of Occupational Exposure Limits, a Committee of the Health Council of the Netherlands, No. 2000/15OSH/148 The Hague, 2005.
  • [7] Clark D.G., Litchfield M.H., Metabolism of Ethylene Glycol Dinitrate and Its Influence on the Blood Pressure of the Rat, Bri. J. Industr. Med., 1967, 29, 321-327.
  • [8] Szilágyi B., Corrosion Inhibitors in Antifreeze Coolants, 44th Int. Petroleum Conference, Bratislava, Slovak Republic, 2009.
  • [9] Schmitt T.M., Muzhe E.S., Determination of 2-Mercaptobenzothiazole, Tolyltriazole and Benzotriazole in Coolant Formulations by Liquid Chromatography, Talanta, 1981, 28, 777-779.
  • [10] Ramirez M.L., Félix-Rivera H., Rivera S.P.H, Thermal-spectroscopic Characterization of Acetone Peroxide and Acetone Peroxide Mixtures with Nitro Compounds, J. Therm. Anal. Calorim., 2010, 102, 549-555.
  • [11] Wu S., Chi J., Wu Y., Huang Y., Chu F., Horng J., Shu C., Charpentier J., Thermal Hazard Analysis of Triacetonetriperoxide (TATP) by DSC and GC/MS, J. Loss Prev. Process Ind., 2012, 25, 1069-1074.
  • [12] Wild R., Collani E.V., Modelling of Explosives Sensitivity. Part 1: The Bruceton Method, Economic Quality Control, 2002, 17.
  • [13] Simpson L.R, Foltz M.F, LLNL Small-scale Drop-hammer Impact Sensitivity,Lawrence Livermore National Laboratory Test, UCRL-ID-119665, 1995.
  • [14] Li M.M., Wang G.X., Guo X.D., Wu Z.W., Song H.Ch., Theoretical Studies on the Structures, Thermodynamic Properties, Detonation Properties, and Pyrolysis Mechanisms of Four Trinitrate Esters, J. Mol. Struct.: THEOCHEM, 2008, 900, 90-95.
  • [15] Brauera B., Dubnikovaa F., Zeiri Y., Kosloff R., Gerbera R.B, Vibrational Spectroscopy of TATP: Anharmonic Fundamentals, Overtones and Combination Bands, Spectrochim. Acta, 2008, 71, 1438-1445.
  • [16] Oxley J.C, Smith L., Brady J.E., Brown A.C., Characterization and Analysis of Tetranitrate Esters, Propellants Explos. Pyrotech., 2012, 37, 629-735.
  • [17] Günther H., Honga Q., Stübeb D., Maierb M., Häringa H., Liebicha H., Simultaneous Analysis of the Di(2-ethylhexyl) Phthalate Metabolites 2-Ethylhexanoic Acid, 2-Ethyl-3-hydroxyhexanoic Acid and 2-Ethyl-3-oxohexanoic Acid in Urine by Gas Chromatography-Mass Spectrometry, J. Chromatogr. B: Biomed. Sci. Appl., 2001, 758, 07-15.
  • [18] Zitrin J., Modern Methods and Application in Analysis of Explosives, Wiley, 1993, p. 310.
  • [19] Fettaka H., Lefebvre M., Investigation of Commercial Precursors for the Synthesis of Liquid Nitroesters, New Trends Res. Energ. Mater., Proc. Semin., 17th, Pardubice,
  • [20] Cooper P.W., Explosives Engineering, WILEY-VCH, 1996, 306.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-9a8d9717-8210-4dad-8b05-c34ba18da0fe
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